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Plasticity of lifelong calorie‐restricted C57BL/6J mice in adapting to a medium‐fat diet intervention at old age
Calorie restriction (CR) is a dietary regimen that supports healthy aging. In this study, we investigated the systemic and liver‐specific responses caused by a diet switch to a medium‐fat (MF) diet in 24‐month‐old lifelong, CR‐exposed mice. This study aimed to increase the knowledge base on dietary...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847878/ https://www.ncbi.nlm.nih.gov/pubmed/29266667 http://dx.doi.org/10.1111/acel.12696 |
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author | Rusli, Fenni Boekschoten, Mark V. Borelli, Vincenzo Sun, Chen Lute, Carolien Menke, Aswin L. van den Heuvel, Joost Salvioli, Stefano Franceschi, Claudio Müller, Michael Steegenga, Wilma T. |
author_facet | Rusli, Fenni Boekschoten, Mark V. Borelli, Vincenzo Sun, Chen Lute, Carolien Menke, Aswin L. van den Heuvel, Joost Salvioli, Stefano Franceschi, Claudio Müller, Michael Steegenga, Wilma T. |
author_sort | Rusli, Fenni |
collection | PubMed |
description | Calorie restriction (CR) is a dietary regimen that supports healthy aging. In this study, we investigated the systemic and liver‐specific responses caused by a diet switch to a medium‐fat (MF) diet in 24‐month‐old lifelong, CR‐exposed mice. This study aimed to increase the knowledge base on dietary alterations of gerontological relevance. Nine‐week‐old C57BL/6J mice were exposed either to a control, CR, or MF diet. At the age of 24 months, a subset of mice of the CR group was transferred to ad libitum MF feeding (CR‐MF). The mice were sacrificed at the age of 28 months, and then, biochemical and molecular analyses were performed. Our results showed that, despite the long‐term exposure to the CR regimen, mice in the CR‐MF group displayed hyperphagia, rapid weight gain, and hepatic steatosis. However, no hepatic fibrosis/injury or alteration in CR‐improved survival was observed in the diet switch group. The liver transcriptomic profile of CR‐MF mice largely shifted to a profile similar to the MF‐fed animals but leaving ~22% of the 1,578 differentially regulated genes between the CR and MF diet groups comparable with the expression of the lifelong CR group. Therefore, although the diet switch was performed at an old age, the CR‐MF‐exposed mice showed plasticity in coping with the challenge of a MF diet without developing severe liver pathologies. |
format | Online Article Text |
id | pubmed-5847878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58478782018-04-01 Plasticity of lifelong calorie‐restricted C57BL/6J mice in adapting to a medium‐fat diet intervention at old age Rusli, Fenni Boekschoten, Mark V. Borelli, Vincenzo Sun, Chen Lute, Carolien Menke, Aswin L. van den Heuvel, Joost Salvioli, Stefano Franceschi, Claudio Müller, Michael Steegenga, Wilma T. Aging Cell Original Articles Calorie restriction (CR) is a dietary regimen that supports healthy aging. In this study, we investigated the systemic and liver‐specific responses caused by a diet switch to a medium‐fat (MF) diet in 24‐month‐old lifelong, CR‐exposed mice. This study aimed to increase the knowledge base on dietary alterations of gerontological relevance. Nine‐week‐old C57BL/6J mice were exposed either to a control, CR, or MF diet. At the age of 24 months, a subset of mice of the CR group was transferred to ad libitum MF feeding (CR‐MF). The mice were sacrificed at the age of 28 months, and then, biochemical and molecular analyses were performed. Our results showed that, despite the long‐term exposure to the CR regimen, mice in the CR‐MF group displayed hyperphagia, rapid weight gain, and hepatic steatosis. However, no hepatic fibrosis/injury or alteration in CR‐improved survival was observed in the diet switch group. The liver transcriptomic profile of CR‐MF mice largely shifted to a profile similar to the MF‐fed animals but leaving ~22% of the 1,578 differentially regulated genes between the CR and MF diet groups comparable with the expression of the lifelong CR group. Therefore, although the diet switch was performed at an old age, the CR‐MF‐exposed mice showed plasticity in coping with the challenge of a MF diet without developing severe liver pathologies. John Wiley and Sons Inc. 2017-12-21 2018-04 /pmc/articles/PMC5847878/ /pubmed/29266667 http://dx.doi.org/10.1111/acel.12696 Text en © 2017 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Rusli, Fenni Boekschoten, Mark V. Borelli, Vincenzo Sun, Chen Lute, Carolien Menke, Aswin L. van den Heuvel, Joost Salvioli, Stefano Franceschi, Claudio Müller, Michael Steegenga, Wilma T. Plasticity of lifelong calorie‐restricted C57BL/6J mice in adapting to a medium‐fat diet intervention at old age |
title | Plasticity of lifelong calorie‐restricted C57BL/6J mice in adapting to a medium‐fat diet intervention at old age |
title_full | Plasticity of lifelong calorie‐restricted C57BL/6J mice in adapting to a medium‐fat diet intervention at old age |
title_fullStr | Plasticity of lifelong calorie‐restricted C57BL/6J mice in adapting to a medium‐fat diet intervention at old age |
title_full_unstemmed | Plasticity of lifelong calorie‐restricted C57BL/6J mice in adapting to a medium‐fat diet intervention at old age |
title_short | Plasticity of lifelong calorie‐restricted C57BL/6J mice in adapting to a medium‐fat diet intervention at old age |
title_sort | plasticity of lifelong calorie‐restricted c57bl/6j mice in adapting to a medium‐fat diet intervention at old age |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847878/ https://www.ncbi.nlm.nih.gov/pubmed/29266667 http://dx.doi.org/10.1111/acel.12696 |
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